p38 MAPK and NF-κB pathways are involved in naphtho[1,2-b] furan-4,5-dione induced anti-proliferation and apoptosis of human hepatoma cells

被引:51
作者
Chiu, Chien-Chih [1 ,3 ]
Chen, Jeff Yi-Fu [1 ,3 ]
Lin, Kuwi-Li [2 ]
Huang, Chi-Jung [1 ]
Lee, Jin-Ching [1 ]
Chen, Bin-Hung [1 ]
Chen, Wan-Yu [1 ]
Lo, Yi-Han [1 ]
Chen, Yi-Lan [1 ]
Tseng, Chih-Hua [2 ]
Chen, Yeh-Long [2 ]
Lin, Shinne-Ren [2 ]
机构
[1] Kaohsiung Med Univ, Dept Biotechnol, Kaohsiung 807, Taiwan
[2] Kaohsiung Med Univ, Dept Med & Appl Chem, Kaohsiung 807, Taiwan
[3] Kaohsiung Med Univ, Ctr Excellence Environm Med, Kaohsiung 807, Taiwan
关键词
p38; MAPK; NF-kappa B; Naphthoquinone; Hepatocellular carcinoma (HCC); ANTITUMOR-ACTIVITY; BCL-2; ACTIVATION; ERK; OVEREXPRESSION; MITOCHONDRIA; INDUCTION; CASPASE-3; CLEAVAGE; POTENT;
D O I
10.1016/j.canlet.2010.02.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Naphtho[1,2-b] furan-4,5-dione (NFD) was investigated for its anti-proliferation effect on human hepatocellular carcinoma (HCC), Hep3B, HepG(2), and Huh-7 cells. The effect of NFD on inhibiting proliferation and apoptosis was correlated with up-regulation of proapoptotic protein and down-regulation of pro-survival proteins. Remarkably, we found that NFD inhibited the nuclear translocation of NF-kappa B, likely accounting for the down-regulation of pro-survival Bcl-2 family. Furthermore, suppression of p38 MAPK activity by a specific inhibitor significantly rescued the cell proliferation inhibited by NFD. These findings suggest that signaling imbalance between p38 MAPK and NF-kappa B by NFD results in the proliferative inhibition and apoptosis of HCC tumor cells. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:92 / 99
页数:8
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